Chemical Structure : ML471
货号: PC-23599Not For Human Use, Lab Use Only.
ML471 is a potent, selective reaction hijacking inhibitor of P.falciparum tyrosine tRNA synthetase (PfTyrRS, PfYRS), inhibits growth of asexual blood stage P. falciparum (3D7 strain) in a 72-h exposure assay with IC50 of 2.8 nM.
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ML471 is a potent, selective reaction hijacking inhibitor of P.falciparum tyrosine tRNA synthetase (PfTyrRS, PfYRS), inhibits growth of asexual blood stage P. falciparum (3D7 strain) in a 72-h exposure assay with IC50 of 2.8 nM.
ML471 has no inhibitory activity against human ubiquitin-activating enzyme (UAE) in vitro.
ML471 exhibits low nanomolar activity against asexual blood stage P. falciparum and potent activity against liver stage parasites, gametocytes and transmissible gametes.
ML471 is well-tolerated and shows single dose oral efficacy in the SCID mouse model of P. falciparum malaria.
分子量 | 388.40 | |
分子式 | C13H20N6O6S | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Xie SC, et al. PLoS Pathog. 2024 Dec 9;20(12):e1012429.
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